Low serum-free oxygen radicals defense level is associated with peripheral arterial stiffness in kidney transplantation patients

Bang Gee Hsu, Chung Jen Lee, Yen Cheng Chen, Guan Jin Ho, Teng Yi Lin, Ming Che Lee

研究成果: 雜誌貢獻文章同行評審

摘要

Oxidative stress is a causative mechanism of vascular alterations resulting in arterial stiffness. The aim of this study was to evaluate the relationship between oxidative stress and arterial stiffness among kidney transplantation (KT) patients. Fasting blood samples were obtained from 70 KT patients. Arterial stiffness was measured by brachial-ankle pulse wave velocity. Oxidative stress was measured by free oxygen radicals testing (FORT) and free oxygen radicals defense (FORD). We found that diabetes (P = 0.005), hypertension (P = 0.001), metabolic syndrome (P = 0.029), age (P = 0.007), KT duration (P = 0.007), waist circumference (P = 0.039), systolic blood pressure (P < 0.001), diastolic blood pressure (P = 0.004), pulse pressure (P = 0.001), triglycerides (P = 0.049), fasting glucose (P = 0.003), insulin (P = 0.011), homeostasis model assessment of insulin resistance (HOMA-IR, P = 0.002), and FORT (P = 0.014) were all higher in the high arterial stiffness group, while HDL-C (P = 0.004) and FORD (P = 0.009) were lower. Multivariate logistic regression analysis of all significant variables showed that FORD level (OR: 0.849, 95% CI: 0.740-0.973, P = 0.019) is inversely associated with arterial stiffness. Logarithmically transformed HOMA-IR (β = -0.280, P = 0.019) was independently associated with FORD levels in KT patients. Our study showed that KT patients with higher serum FORT level and lower FORD level had high arterial stiffness. Low serum FORD level is an independent predictor of peripheral arterial stiffness in KT patients. Among these KT patients, logarithmically transformed HOMA-IR is negatively associated with serum FORD level.

原文英語
頁(從 - 到)10698-10706
頁數9
期刊International Journal of Clinical and Experimental Pathology
9
發行號10
出版狀態已發佈 - 2016
對外發佈

ASJC Scopus subject areas

  • 病理學與法醫學
  • 組織學

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